dc.creatorZanocco Loyola, Antonio
dc.creatorLemp Miranda, Else
dc.creatorPizarro, Nancy
dc.creatorDe la Fuente, Julio
dc.creatorGünther Sapunar, Germán
dc.date.accessioned2018-12-20T15:20:36Z
dc.date.available2018-12-20T15:20:36Z
dc.date.created2018-12-20T15:20:36Z
dc.date.issued2001
dc.identifierJournal of Photochemistry and Photobiology A: Chemistry, Volumen 140, Issue 2, 2018, Pages 109-115
dc.identifier10106030
dc.identifier10.1016/S1010-6030(01)00393-8
dc.identifierhttps://repositorio.uchile.cl/handle/2250/158836
dc.description.abstractDetection of O2(1Δg) phosphorescence emission, λmax=1270nm, following laser excitation and steady state methods were employed to determine both the total constant, kT LID, and the chemical reaction rate constants, kR LID, for reaction between the anaesthetic lidocaine and singlet oxygen in several solvents. Values of kT LID range from 0.20±0.09×106M-1s-1 in trifluoroethanol to 45.8±2.40×106M-1s-1 in N,N-dimethylacetamide. Values of kR LID are at least one order of magnitude lower than kT LID values in a given solvent. Solvent effect on quenching rates shows that reaction mechanism involves formation of a charge transfer exciplex. Correlation of kT LID values with solvent parameters does not follow that observed for a typical tertiary amine such as triethylamine. Although kT LID values are lower in hydrogen bond donor solvents, this solvent effect is significantly smaller than that for triethylamine, and no expected decrease in lidocaine reactivity with change from aprotic to protic sol
dc.languageen
dc.publisherElsevier
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceJournal of Photochemistry and Photobiology A: Chemistry
dc.subjectLidocaine
dc.subjectLSER
dc.subjectPhotosensitization
dc.subjectSinglet oxygen
dc.subjectSolvent effect
dc.subjectTLSER
dc.titleSolvent effects on the sensitized photoxygenation of lidocaine
dc.typeArtículo de revista


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